Are you looking for an exciting opportunity to lead complex engineering projects in a growing, international pharmaceutical company? At ALK, we are on a mission to improve the lives of people living with allergies, and we are seeking a driven and structured Project Manager to join our team.In this role, you'll take ownership of projects and ensure their implementation across production, utilities, and facilities areas. This is a hands‑on, cross‑functional role for a delivery‑focused professional who thrives on managing scope, cost, and timelines, champions GMP and compliance excellence, drives continuous improvement, and enjoys collaborating with stakeholders and vendors alike.Your key responsibilities:The Project Manager leads projects related to pharmaceutical production, utilities, and facilities, ensuring delivery on time and on budget while meeting all quality and compliance expectations. Key responsibilities include:- Project Leadership - Lead projects and collaborate with all stakeholders in the scoping, design, sourcing, installation, commissioning, qualification, and handover of equipment for the production areas.- Requirements & Specifications - Define equipment requirements and specifications based on process, safety, quality, and customer needs. Establish the general automation requirements for manufacturing, QA, and QC equipment.- Technology Evaluation - Evaluate, or assist in evaluating, the technology necessary to support project requirements.- Budget & Cost Management - Assist in determining and managing the budget required to support project requirements,



ensuring delivery on time and on cost.- Vendor & Subcontractor Management - Manage the efforts of subcontractors and vendors to ensure the correct job priorities and schedules are met, whether delivered by internal or external crews.- Quality & Compliance - Take accountability for the quality and compliance aspects of the assigned activities, performing the required actions (risk analysis, documentation, inspection participation, observation responses, SOPs, etc.).Your profile:- Degree in Science or Engineering.- Candidates should have prior experience in a similar role, ideally within a GMP pharmaceutical/biotech environment.- Demonstrated capability of working within GMP frameworks.- Knowledge of Quality Systems and Validation standards, policies, procedures, and methodologies.- Fluent Spanish and English; excellent technical writing and communication skills.Your skills and attributes:- Structured and delivery-focused, comfortable managing multiple projects in parallel.- Strong stakeholder management; able to influence and coordinate internal teams and external vendors.- Meticulous attention to detail with a pragmatic, risk‑based approach to compliance.- Confident problem‑solver with strong organisational and planning skills.- Location: C/ Miguel Fleta, 19 (Madrid, Spain).- Reporting line: Projects & Qualification Manager.- Work pattern: Regular day shift with a versátil schedule.We provide:- Competitive salary package.- Stable employment and a positive work environment.- A comprehensive benefits package including health insurance, subsidized meals, and a pension plan.#J-18808-Ljbffr

📌 Project Manager (Madrid)
🏢 Alk-Abelló, A/S
📍 Madrid